Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota

Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide...

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Veröffentlicht in:International journal of biological macromolecules 2024-11, Vol.280 (Pt 4), p.136039, Article 136039
Hauptverfasser: Chen, Yanlan, Huang, Junyuan, Wang, Huaixu, Cui, Haohui, Liang, Zizhao, Huang, Darong, Deng, Xinyu, Du, Bing, Li, Pan
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container_end_page
container_issue Pt 4
container_start_page 136039
container_title International journal of biological macromolecules
container_volume 280
creator Chen, Yanlan
Huang, Junyuan
Wang, Huaixu
Cui, Haohui
Liang, Zizhao
Huang, Darong
Deng, Xinyu
Du, Bing
Li, Pan
description Renal fibrosis is a common pathway involved in the progression of various chronic kidney to end-stage diseases, posing a substantial global public health challenge in the search for effective and safe treatments. This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. In addition, SISP altered the intestinal flora imbalance in HSD mice by reducing the relative abundance of the genera, Akkermansia, Faecalibaculum, and unidentified_Ruminococcaceae, and reversing the decline in the levels of the genera, Lactobacillus and Bacteroides. In conclusion, SISP is a promising nutraceutical for renal fibrosis management.
doi_str_mv 10.1016/j.ijbiomac.2024.136039
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This study investigated the effects and mechanisms of sacha inchi shell polysaccharide (SISP) on renal fibrosis induced by a high-salt diet (HSD) in mice. By analysing kidney-related protein pathways and the structure of gut microbiota, we found that SISP significantly reduced urinary protein levels induced by a HSD from 41.08 to 22.95 μg/mL and increased urinary creatinine from 787.43 to 1294.50 μmol/L. It reduced renal interstitial collagen fibres by 11.30 %, thereby improving the kidney function. SISP lowered the mRNA expression of TGF-B1, fibronectin, α-SMA, Smad2/3, and TGFBRII, leading to decreased protein levels of TGF-β1, p-Smad2/3, p-TGFβRII, fibronectin, α-SMA, p-Smad2/3/Smad2/3, and p-TGFβRII/TGFβRII. These changes blocked downstream transcription in the TGF-β1/Smad signalling pathway, thereby attenuating renal fibrosis in HSD mice. 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subjects Animals
Bacteroides
collagen
creatinine
dietary supplements
fibronectins
Fibrosis
Gastrointestinal Microbiome - drug effects
gene expression
intestinal microorganisms
Kidney - drug effects
Kidney - metabolism
Kidney - pathology
Kidney Diseases - drug therapy
Kidney Diseases - metabolism
Kidney Diseases - pathology
kidneys
Lactobacillus
Male
Mice
Polysaccharides
Polysaccharides - pharmacology
public health
Renal fibrosis
renal function
Signal Transduction - drug effects
Smad Proteins - metabolism
TGF-β1
Transforming Growth Factor beta1 - metabolism
title Polysaccharides from Sacha Inchi shell reduces renal fibrosis in mice by modulating the TGF-β1/Smad pathway and intestinal microbiota
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